FIELD OF THE INVENTION
[0001] The present invention relates to the field of pet food. More specifically, the present
invention is related to palatability-enhancing animal digests for use in pet food.
BACKGROUND OF THE INVENTION
[0002] Protein hydrolysates are standard components of pet food, to which they typically
confer palatability.
[0003] Protein hydrolysis can generally be achieved by physical (heat and shear) or chemical
(acid or enzymes) means. However, enzymatic hydrolysis is the most widespread method
for hydrolyzing proteins in the food industry, in particular because enzymes enable
to obtain hydrolysates (or digests) of interest for nutritional and/or organoleptic
purposes.
[0004] Proteolytic enzymes are proteases or peptidases which can be identified:
- on the basis of the key amino acid involved in the active site mechanisms of the enzyme:
serine; carboxyl; sulfhydryl; or metallo, and/or
- by the relative pH range in which they are active: acid; neutral; or alkaline; and/or
- based on their hydrolytic abilities: an endoprotease or endopeptidase cuts between
amino acids on the interior of a protein or a peptide, whereas an exoprotease or exopeptidase
cleaves off amino acids at the ends of a protein or a peptide.
[0005] As examples of common endoproteases, one can cite: chymosin which is a highly specific
endoprotease; pepsin having relatively broad specificity but cleaving preferably bonds
involving Phe, Met, Leu, and Tryp residues; neutral proteases such as trypsin which
is a highly specific endoprotease that cleaves bonds between Arg or Lys residues and
the subsequent amino acid; papain and bromelain that are non-specific sulfhydryl endopeptidases;
alkaline proteases such as subtilisin which is quite non-specific; and the like.
[0006] In food industry, it is well-known that protein hydrolysis affects biological, physical,
and chemical properties, as well as food processing, and that this may be advantageous
or not. On the one hand, hydrolysis generally improves solubility, as well as heat
and pH resistance due to low molecular weight distribution. On the other hand, it
typically increases osmolarity and reduces chemical stability. Moreover, depending
on the enzymes, the protein sources and/or the reaction conditions, palatability may
be reduced owing to, e.g., production of bitter peptides. It is thus essential to
adequately determine the enzymes, protein sources and reaction conditions (e.g., enzyme
concentration and reaction time) to achieve a specific technical effect of the resulting
digests.
[0007] Pet food manufacturers often use liver or viscera of poultry and animal by-products
as protein sources in pet food production. Among viscera, some (e.g., gut) are advantageously
rich in proteolytic enzymes so that they require very little, if any, additional protease
for hydrolyzing proteins. When using animal organs as protein sources, it is also
possible to take advantage of endogenous proteolytic enzymes. However, among these
enzymes, exoproteases are often too highly represented to produce an appropriate digest.
Thus, the meat source is usually ground and treated with appropriately selected enzymes
to provide a high yield of flavoring peptides. In addition, because flavor preferences
differ from one pet species to another, pet food manufacturers need to select enzymes,
protein sources, and hydrolysis conditions, that enable to obtain high yields of digests
having the desirable palatability properties. Further to optimizing palatability,
the chosen proteases should be adapted to "friendly" processing conditions such as
moderate enzyme concentrations as well as temperature ranges that help to limit manufacturing
costs and to prevent bacterial growth, respectively.
[0008] In pet food industry, palatability enhancers (PEs) are extremely useful, if not necessary,
for animal consumption. Many pets, and cats in particular, may even refuse to eat
extruded pet food that has not been treated with PEs. Pet foods typically contain
flavor compositions to increase the palatability thereof and to make them appealing
to pets.
[0009] PEs are liquid or dry compositions, that can be used alone or in combination. Some
PEs are applied to the outer surface of the pet food (coating) whereas other PEs are
incorporated into the pet food material (inclusion).
[0010] Flavoring protein hydrolysates are widely used as PEs. For instance, International
patent application published under No.
WO2011/043828 discloses methods for enhancing the palatability of animal digests useful as PEs.
These methods comprise adding anti-gelling agents to animal digests while adjusting
the pH to a value optimal for proteases used to hydrolyze viscera proteins. Also,
International patent application published under No.
WO2009/095417 describes methods for enhancing the palatability of pet foods by using a PE prepared
by sequential steps of hydrolysis with proteases and lipases.
[0011] There is however a continuing effort to develop processing and formulations which
improve the palatability of pet food while maintaining its nutritional value.
SUMMARY OF THE INVENTION
[0012] The present invention concerns a method for preparing an animal digest having enhanced
palatability, comprising:
- a) providing an animal viscera;
- b) contacting said animal viscera with at least one alkaline endopeptidase in an appropriate
amount;
- c) allowing said alkaline endopeptidase to hydrolyze said animal viscera for a suitable
period of time;
- d) thermally treating the thus obtained digest product to inactivate said alkaline
endopeptidase; and
- e) obtaining said animal digest having an appropriate degree of hydrolysis and exhibiting
enhanced palatability, as claimed.
BRIEF DESCRIPTION OF THE FIGURES
[0013] The present invention is illustrated by reference to the following accompanying figures:
- Figure 1: Flowchart representing various embodiments of the method according to the
present invention. Essential steps a), b), c), d), and e) are represented in continuous
line; optional steps a1), c1), d1), d2), d3), d4), d5), and d6) are represented in
dotted line.
- Figure 2: Graphic representations of the degree of hydrolysis (DH) as a function of
the alkaline endopeptidase amount (E) and of the time of the hydrolysis reaction (T).


DETAILED DESCRIPTION OF THE INVENTION
DEFINITIONS
[0014] Unless specifically stated otherwise, percentages are expressed herein by weight
of a liquid digest product obtained after the thermal treatment step d) of the method
of the present invention. This liquid digest product results from said step d). Alternatively,
if step d) is followed by a filtrating step d1), then percentages will be expressed
by weight of a liquid digest product obtained from said step d1). Yet alternatively,
if said step d) or d1) is followed by a cooling down step d2), then percentages will
be expressed by weight of a liquid digest product obtained from said step d2) (see
Fig. 1).
[0015] In the present disclosure, ranges are stated in shorthand, so as to avoid having
to set out at length and describe each and every value within the range. Any appropriate
value within the range can be selected, where appropriate, as the upper value, lower
value, or the terminus of the range. For example, a range of 0.1-1.0 represents the
terminal values of 0.1 and 1.0, as well as the intermediate values of 0.2, 0.3, 0.4,
0.5, 0.6, 0.7, 0.8, 0.9, and all intermediate ranges encompassed within 0.1-1.0, such
as 0.2-0.5, 0.2-0.8, 0.7-1.0, etc.
[0016] As used throughout, the singular form of a word includes the plural, and vice versa,
unless the context clearly dictates otherwise. Thus, the references "a", "an", and
"the" are generally inclusive of the plurals of the respective terms. For example,
reference to "a method" or "a food" includes a plurality of such "methods" or "foods".
Similarly, the words "comprise", "comprises", and "comprising" are to be interpreted
inclusively. Likewise the terms "include", "including" and "or" should all be construed
to be inclusive. All these terms however have to be considered as encompassing exclusive
embodiments that may also be referred to using words such as "consist of".
[0017] The methods and compositions and other embodiments exemplified here are not limited
to the particular methodologies, protocols, and reagents that are described herein
because, as the skilled artisan will appreciate, they may vary.
[0018] Unless defined otherwise, all technical and scientific terms, terms of art, and acronyms
used herein have the meanings commonly understood by the skilled artisan in the field(s)
of the invention, or in the field(s) where the term is used. Although any compositions,
methods, articles of manufacture, or other means or materials similar or equivalent
to those described herein can be used in the practice of the present invention, the
preferred compositions, methods, articles of manufacture, or other means or materials
are described herein.
[0019] The term "about" as used herein when referring to a measurable value such as an amount,
a temporal duration, and the like, is meant to encompass variations of ±10%, more
preferably ±5%, even more preferably ±3% from the specified value, as such variations
are appropriate to reproduce the disclosed methods and products.
[0020] The term "palatability" means a relative preference of an animal for one food composition
to another. Palatability refers to the overall willingness of an animal to eat a certain
food. Advantageously but not necessarily, palatability further refers to the capacity
of the eaten food to satisfy the animal. Whenever an animal shows a preference, for
example, for one of two or more foods, the preferred food is more "palatable", and
has "enhanced palatability". The relative palatability of one food compared to one
or more other foods can be determined, for example, in side-by-side, free-choice comparisons,
e.g., by relative consumption of the foods, or other appropriate measures of preference
indicative of palatability. It can advantageously be determined by a standard testing
protocol in which the animal has equal access to both compositions such as a test
called "two-bowl test" or "versus test" (see below). Such preference can arise from
any of the animal's senses, but typically is related to,
inter alia, taste, aroma, flavour, texture, smell and/or mouth feel.
[0021] A pet food stated herein to have "enhanced palatability" is one for which a pet exhibits
preference relative to a control composition. Advantageously, a pet food having enhanced
palatability is appealing or pleasing not just to pets, but to pet owners as well.
[0022] The terms "palatability enhancers" (PEs), "palatants", "flavours", "palatability
agents", "appetizing factors", "flavour compositions", "palatability-enhancing compositions",
"flavour enhancers", and any other similar terms mean any material that enhances the
palatability of a food composition to an animal. A PE may be a single material or
a blend of materials, and it may be natural, processed or unprocessed, synthetic,
or part of natural and part of synthetic materials. Typically, a PE for animal food
is an edible composition that provides an aroma, taste, aftertaste, smell, mouth feel,
texture, and/or organoleptic sensation that is appealing or pleasing to the target
animal.
[0023] For example, a PE may contribute to initial food appeal by its smell and/or to continued
consumption by its smell but also by its taste and/or its aftertaste, and/or its mouthfeel,
and/or its texture. "Initial appeal" is an aspect of palatability that induces an
animal to initially taste or try a food, and that can be measured by the criteria
"first choice" or "first food consumed". "Continued consumption" is an aspect of palatability
that induces an animal to continue consuming a food that has been initially only tasted
or tried.
[0024] The term "animal" is used in a general sense and means a human or other animal that
may choose an edible composition based upon its palatability, including avian, bovine,
canine, equine, feline, lupine, murine, ovine, and porcine animals, thus encompassing
pets.
[0025] The present invention preferably concerns pets.
[0026] The terms "pet" and "companion animal" are synonymous and mean any domesticated animal
including, without limitation, cats, dogs, rabbits, guinea pigs, ferrets, hamsters,
mice, gerbils, birds, horses, cows, goats, sheep, donkeys, pigs, and the like.
[0027] In the context of the present invention, pets such as dogs and cats are preferred.
However, although the present disclosure is focused on dogs and cats, the invention
can be adapted for use with other classes of companion animals. If desired, the invention
can be tested to evaluate its suitability for use with different classes of animals
that may be considered as companion animals.
[0028] The term "food" as used herein means a product or composition that is intended for
ingestion by an animal and provides at least one nutrient to the animal. The term
"food" includes any food, feed, snack, food supplement, treat, toy (chewable and/or
consumable toys), meal substitute, or meal replacement. "Food" encompasses such products
in any form, solids, liquids, gels, or mixtures or combinations thereof. Thus, beverages
of any type are clearly encompassed within the term "food."
[0029] The term "pet food" means a composition intended for consumption by a pet.
[0030] There are three main categories or classes of pet foods depending on their moisture
content, which is either low or medium or high:
- dry or low moisture-containing products (having less than about 15% moisture): they
usually produce a crunching sound when chewed by a pet; they are generally highly
nutritious, may be inexpensively packaged (e.g., in bags or boxes), and are highly
convenient to store and use; however, they are typically the least palatable;
- canned or wet or high moisture-containing products (having more than about 50% moisture):
typically high meat-containing products, they are generally considered as the most
palatable to pets; they are usually costly to produce and package (mainly in cans);
- semi-moist or semi-dry or soft dry or soft moist or intermediate or medium moisture-containing
products (having from about 15 to about 50% moisture): usually packaged in appropriate
bags or boxes, they are commonly less palatable than canned foods but more palatable
than dry foods.
[0031] Nutritionally-balanced pet foods are widely known and used in the art.
[0032] A "nutritionally-complete", "nutritionally-balanced" or "complete and nutritionally-balanced
food" is one that contains all known required nutrients for the intended recipient
or consumer of the food, in appropriate amounts and proportions based, for example,
on recommendations of recognized or competent authorities in the field of companion
animal nutrition. Such foods are therefore capable of serving as a sole source of
dietary intake to maintain life or promote production, without the addition of supplemental
nutritional sources.
[0033] The term "kibble" used herein refers to particulate chunks or pieces formed by either
a pelleting or extrusion process. Typically, kibbles are produced to give dry and
semi-moist pet food. The pieces can vary in sizes and shapes, depending on the process
or the equipment. For instance, kibbles can have spherical, cylindrical, oval, or
similar shapes. They can have a largest dimension of less than about 2 cm for example.
[0034] The term "chunk-in-"X" products" mean herein all edible foodstuffs comprising chunks
in a preparation (said preparation being "the X preparation"). Classical examples
thereof are chunk-in-jelly products, chunk-in-gravy products, and the like. This category
of "chunk-in-X" products encompasses also edible forms other than chunks that may
be contained in the X preparation such as a jelly, a gravy, and the like. For instance,
other forms than chunks may be sliced products, grated products, etc.
[0035] The term "loaf" used herein refers to edible foodstuffs obtained as moist products,
and includes terrines, pates, mousses, and the like.
[0036] The term "food supplement" or "dietary supplement" or "supplement" means a product
that is intended to be ingested in addition to the normal animal diet. Dietary supplements
may be in any form, e.g., solid, liquid, gel, tablets, capsules, powder, and the like.
Preferably they are provided in convenient dosage forms. In some embodiments, they
are provided in bulk consumer packages such as bulk powders, liquids, gels, or oils.
In other embodiments, supplements are provided in bulk quantities to be included in
other food items such as snacks, treats, supplement bars, beverages, and the like.
Patatability-enhancing compositions can be used to improve palatability of dietary
supplements in the same manner as they are used to improve palatability of nutritionally-balanced
foods.
[0037] The term "treat" (or "biscuit") means any food item that is designed to be fed to
a pet, preferably at non-meal time, by the owner to help, promote or sustain a bonding
process between a pet and its owner. Examples of treats for dogs are bones. Treats
may be nutritional or not. Treats often contain palatability enhancers in a manner
comparable to nutritionally-balanced foods.
[0038] "Toys" include, for example chewable toys. Examples of toys for dogs are artificial
bones. Toys further include partially consumable toys (e.g., comprising plastic components)
or fully consumable toys (e.g., rawhides).
[0039] The term "animal digest" means herein material which results from chemical and/or
enzymatic hydrolysis of clean, undecomposed animal tissue. In some embodiments, an
animal digest as used herein is fully consistent with the definition promulgated by
the Association Of American Feed Control Officials, Inc. (AAFCO). Animal digest is
preferably derived from animal tissues as well as fish tissues, excluding hair, horns,
teeth, hooves, and feathers. The skilled artisan will appreciate that while such tissues
are not preferred, trace amounts might be found unavoidably even under good manufacturing
practices. Also not included are visceral contents or foreign or fecal matter, although
trace contaminant amounts are sometimes present. An animal digest may be dried or
not. Typically, examples of animal digests are:
- digest of poultry (or pork, beef, sheep, lamb, fish, etc.): material from poultry
(pork, beef, etc.) which results from chemical and/or enzymatic hydrolysis of clean
and undecomposed tissue;
- digest of pork (or beef, sheep, lamb, fish, etc.) by-products: material from pork
(beef, etc.) which results from chemical and/or enzymatic hydrolysis of clean and
undecomposed tissue from non-rendered clean parts from cattle (pigs, sheep, lamb,
etc.), other than meat and bones, for example lungs, spleen, kidneys, brain, livers,
blood, optionally partially-defatted low-temperature fatty tissue, and stomachs and
intestines, freed of their contents;
- digest of poultry by-products: material which results from chemical and/or enzymatic
hydrolysis of clean and undecomposed tissue from non-rendered clean parts of poultry,
other than meat and bones, such as livers, hearts, heads, feet, and viscera. As used
herein, "poultry" encompasses any species or kind of bird, preferably chicken, turkey,
duck, and the like; and
- digest of fish by-products: material which results from chemical and/or enzymatic
hydrolysis of clean and undecomposed tissue from non-rendered clean parts from fish,
other than meat and bones. As used herein, "fish" encompasses any species or kind
of fish or crustaceans or molluscs, preferably tuna, salmon, cod, hake, sardine, shrimp,
squid, and the like.
[0040] Animal digests may also be referred to as "animal products" or "animal by-products",
all these terms being used herein as synonymous.
[0041] In the context of the present invention, however, animal digests are obtained by
enzymatically hydrolysing animal viscera.
[0042] As used herein, the term "animal viscera" or "viscera" means animal and fish tissues
other than meat, fish flesh, and bones, that are useful for producing animal digests
(including fish digests) as defined above. Animal viscera (including fish viscera)
as used herein are preferably ground. Advantageously, one or more pet food ingredients
(as defined below, e.g. preservatives such as anti-oxidants) may be added to said
(preferably ground) animal viscera.
[0043] As used herein, a "pet food ingredient" is any compound, composition or material
that is suitable for pet consumption. Non-limiting examples of pet food ingredients
are PEs, animal digests, nitrogen compounds (e.g., proteins, peptides, and amino acids),
grains, carbohydrates, fats or lipids, nutrients, preservatives including anti-oxidants,
surfactants, texturing or texturizing or stabilizing agents, colouring agents, inorganic
phosphate compounds, prebiotics, probiotics, etc.
[0044] As used herein, a "palatability-enhancing composition ingredient" is any compound,
composition or material that is suitable for pet consumption. Nonlimiting examples
of palatability-enhancing composition ingredients are animal digests, nitrogen compounds
(e.g., proteins, peptides, and amino acids), carbohydrates, fats or lipids, nutrients,
preservatives including anti-oxidants, surfactants, texturing or texturizing or stabilizing
agents, inorganic phosphate compounds, prebiotics, probiotics, etc. Ingredients may
be comprised as such in the palatability-enhancing composition, or they can be contacted
into the composition and react
in situ for producing transformed materials that are also encompassed by the term "palatability-enhancing
composition ingredient". Examples of ingredients that react together in the composition
are, without limitation, nitrogen compounds and carbohydrates, so as to obtain transformed
materials such as Maillard reaction-resulting products, and the like.
[0045] The term "endopeptidase" or "endoprotease" means any proteolytic enzyme that catalyzes
the cleavage of internal bonds in a peptide or a protein.
[0046] The term "alkaline endopeptidase" or "alkaline endoprotease" means any endopeptidase
or endoprotease having an optimal hydrolyzing activity at a pH equal to or greater
than about 7.0. Such an enzyme is preferably active at a pH from about 7.0 to about
10.0.
[0047] "Proteins" or "polypeptides" include all conventional protein sources that are compatible
for animal consumption, especially plant or vegetable proteins, animal proteins, and
microbial proteins (e.g., yeast).
[0048] Examples of animal proteins are casein, albumin, animal digests, poultry meal, meat
meal, bone meal, fish meal, and the like.
[0049] Examples of vegetable proteins are corn gluten, soy protein, soy flour, hydrolyzed
vegetable protein (HVP), and the like.
[0050] The term "yeast" herein refers to any yeast, preferably inactive, as well as to yeast
by-products that are compatible with compositions for animal consumption. Yeasts are
well known in the art as being protein-rich. Yeasts include, without limitation, brewer's
yeast, baker's yeast, torula yeast, molasses yeast, and the like. Yeast by-products
include, without limitation, yeast extracts, yeast hydrolysates, yeast autolysates,
cream yeasts, etc.
[0051] The term "amino acid" means a molecule containing both an amino group and a carboxyl
group. In some embodiments, the amino acids are α-, β-, γ- or δ-amino acids, including
their stereoisomers and racemates.
[0052] As used herein, the terms "nitrogen compound" encompass the twenty known natural
amino acids, as well as amino acid sequences, i.e., peptides, oligopeptides, and proteins
or polypeptides. Also are included all compounds containing nitrogen from any sources
that are acceptable for use in pet foods. Appropriate nitrogen compounds can be chosen
from any nitrogen compounds containing sulfur that are acceptable for use in pet foods,
such as sulfur-containing amino acids (e.g., methionine, cystine, cysteine), glutathione;
other amino acids such as glycine, alanine, glutamic acid, and the like; as well as
other compounds such as HVPs, yeast autolysates, yeast extracts, yeast hydrolysates;
and combinations thereof.
[0053] Examples of grains are corn, milo, alfalfa, wheat, barley, rice, soy, and the like.
[0054] Examples of carbohydrates include dextrose, fructose, sucrose, polysaccharides, fibers,
starches, and the like. Preferably, carbohydrates are or contain reducing sugars.
[0055] Preferably, "reducing sugars" are chosen from hexoses, pentoses, glucose, fructose,
xylose, ribose, arabinose, starch hydrolysates, and the like, as well as combinations
thereof.
[0056] Examples of fats include tallow, oils, from any origin such as animal, plant (including
vegetable), or marine oils. Plant oils which are available in large quantities are
typically canola oil, soybean oil, corn oil, olive oil, sunflower oil, linseed oil,
palm oil, safflower oil, and the like, as well as by-products thereof. Typical animal
fats are tallow, lard, poultry fat, and the like, as well as by-products thereof.
Marine oils are typically tuna oil, sardine oil, salmon oil, anchovy oil, fish oil,
and the like, as well as by-products thereof. Also are encompassed herein the fats
that are derived from animal, plant, marine sources, or that are produced by animals
and plants.
[0057] Examples of nutrients include, without limitation, vitamins, minerals and electrolytes,
such as vitamins A, C, E, B12, D3, folic acid, D-biotin, cyanocobalamin, niacinamide,
thiamine, riboflavin, pyridoxine, menadione, betacarotene, calcium pantothenate, choline,
inositol, calcium, potassium, sodium, zinc, iron, manganese, copper, iodine, and the
like.
[0058] "Preservatives" are in particular used for ensuring a long shelf life of a food product
or a food composition. Preservatives comprise natural or synthetic anti-oxidants (such
as BHA, BHT, propyl gallate, octyl gallate, tocopherols, rosemary extracts, and the
like); as well as sorbic acid or sorbic salts (e.g., potassium sorbate), and other
acids like phosphoric acid and the like. "Surfactants" are molecules that are surface
active. They typically have a hydrophilic portion (e.g., one or more head groups)
and a hydrophobic (or lipophilic) portion (e.g., one or more tails). They are classified
in various ways, for example according to their hydrophilic-lipophilic balance (HLB).
They can also or alternatively be classified as non-ionic, ionic or zwitterionic compounds
based on the presence or absence of formally-charged in the head group(s). Surfactants
are well-known in the art. One can cite, for example, Tween
® surfactants. Surfactants include, without limitation, emulsifiers and wetting agents.
In some instances, the terms "surfactants" and "emulsifiers" can be used interchangeably.
[0059] The term "inorganic phosphate compound" as used herein means a chemical compound
comprising at least one phosphorus atom. This chemical compound may be natural or
synthetic, ionized or not.
[0060] "Inorganic pyrophosphates" or "pyrophosphates" include alkali metal pyrophosphates,
encompassing monoalkali metal pyrophosphates and polyalkali metal pyrophosphates.
[0061] The formula M
xH
yP
nO
3n+1 when n=2 is the general formula for alkali metal pyrophosphates. When M is a univalent
metal, then x+y=n+2. When M is a divalent metal, then x+y=n. Univalent metal pyrophosphates
and divalent metal pyrophosphates can be used herein.
[0062] Examples of monoalkali metal pyrophosphates include sodium trihydrogen pyrophosphate,
potassium trihydrogen pyrophosphate, calcium hydrogen pyrophosphate, barium hydrogen
pyrophosphate, magnesium hydrogen pyrophosphate.
[0063] Polyalkali metal pyrophosphates encompass dialkali metal pyrophosphates, trialkali
metal pyrophosphates, tetralkali metal pyrophosphates, etc.
[0064] Examples of dialkali metal pyrophosphates are disodium dihydrogen pyrophosphate,
dipotassium dihydrogen pyrophosphate, dicalcium pyrophosphate, dibarium pyrophosphate,
dimagnesium pyrophosphate, dimanganese pyrophosphate, dizinc pyrophosphate.
[0065] Trialkali metal pyrophosphates are, for example, trisodium hydrogen pyrophosphate,
tripotassium hydrogen pyrophosphate.
[0066] Pyrophosphates may_be anhydrous or hydrated.
[0067] "Polyphosphates" have the formula M
xH
yP
nO
3n+1 where n is 3, 4, 5,...
[0068] Examples of polyphosphates are tripolyphosphates, pentapolyphosphates, and hexapolyphosphates.
[0069] Tripolyphosphates include sodium tripolyphosphate, potassium tripolyphosphate, calcium
tripolyphosphate, and magnesium tripolyphosphate.
[0070] Hexapolyphosphates include. sodium hexapolyphosphate, potassium hexapolyphosphate,
calcium hexapolyphosphate, and magnesium hexapolyphosphate.
[0071] Examples of monophosphates include monosodium monophosphate, disodium monophosphate,
trisodium monophosphate, monopotassium monophosphate, dipotassium monophosphate, tripotassium
monophosphate, adenosine monophosphate (AMP), guanosine monophosphate (GMP), inosine
monophosphate (IMP), uridine monophosphate (UMP), cytidine monophosphate (CMP).
[0072] A "texturing agent" or "texturizing agent" or "stabilizing agent" is an ingredient
that affects the texture or the mouthfeel of an edible product, e.g., a component
that increases the viscosity of an edible product.
[0073] A "colouring agent" means herein any substance of natural origin or any synthetic
colour that is suitable (preferably certified) for use in pet food. Colouring agents
are useful to,
inter alia, compensate for colour changes during processing or to give an appetizing colour to
an edible product.
[0074] "Probiotics" are live microorganisms that have, upon ingestion, a beneficial effect
on a host animal by improving its intestinal microbial balance. Thereby, probiotics
beneficially affect the host animal by maintaining its health and/or safety and/or
well-being; and/or by preventing and/or treating specific medical conditions. The
probiotics are given to facilitate a process whereby the endogenous anaerobic flora
limits the concentration of potentially harmful (mostly aerobic) bacteria in the digestive
tract. Examples of appropriate probiotics for use in pet food are, without limitation,
lactic acid bacteria such as
Lactobacillus spp.,
Lactococcus spp.,
Streptococcus spp.; as well as other types of bacteria.
[0075] "Prebiotics" are non-digestible food ingredients that beneficially affect an host
animal by selectively stimulating the growth and/or the activity of microorganisms
in the digestive tract, thereby favouring maintenance and/or improvement of the host
animal's health and/or safety and/or well-being. Examples of prebiotics include fructooligosaccharides
(FOS), xylooligosaccharides (XOS), galactooligosaccharides (GOS), and manooligosaccharides.
[0076] A "thermal reaction" is, according to the present invention, a reaction obtained
by combining at an elevated temperature, at least one carbohydrate, preferably a reducing
sugar, and at least one nitrogen compound. Such a reaction may actually include various
concomitant and/or successive reactions, including, e.g., Maillard reaction(s).
[0077] The terms "thermal treatment" as referred to in step d) of the method of the present
invention encompass heat treatments to inactivate enzymes, that can advantageously
be performed concomitantly with thermal reactions as defined above.
[0078] It is thus meant herein by the term "Maillard ingredient(s)", one or more carbohydrates,
preferably reducing sugars; and/or one or more nitrogen compounds. Indeed, Maillard
ingredients are ingredients used to achieve one or more thermal reactions as defined
above.
[0079] As used herein, the term "carrier" means "carrier for concentrating" or "carrier
for drying", and encompasses conventional compounds that are well-known in the art.
Examples thereof are microbial proteins (e.g., yeasts), animal proteins, vegetable
proteins, carbohydrates (e.g., maltodextrin, cyclodextrin), as well as minerals or
inorganic compounds, including inorganic phosphate compounds as defined above.
[0080] Since it is difficult, or even impossible, to determine the exact composition of
protein hydrolysates, manufacturers rather commonly use undirect parameters such as
the degree of hydrolysis (DH) of peptide bonds of proteins. DH is represented by the:
(i) ratio of amino nitrogen over total nitrogen (AN/AT Ratio) in the resulting hydrolysate;
(ii) presence of amines in the hydrolysate; and (iii) osmolarity of the hydrolysate.
Many conventional methods can be used to determine the DH. Methods used in the food
industry, and more specifically in the pet food industry, for quantifying the DH are
typically based on one of the following principles: (1) determination of soluble nitrogen
in the presence of a precipitating agent such as trichloroacetic acid (TCA); or (2)
determination of free alpha amino groups by colorometric methods (e.g., titration
with trinitrobenzenesulfonic acid, TNBS), or pH titration of the released protons.
TCA-soluble nitrogen may be determined by the Kjeldhal assay (A.O.A.C. 1995) or the
Biuret reaction (Hung et al. 1984). Such methods are described in detail in Silvestre
(1997). Alternatively, DH may advantageously be determined by an OPA (o-phthaldialdehyde)-based
method as described below (Nielsen, 2001).
[0081] "Coating", as used herein, refers to the topical deposition of the palatability-enhancing
composition onto the surface of the basal food composition, such as by spraying, dusting,
and the like.
[0082] "Inclusion" as used herein, refers to the addition of the palatability-enhancing
composition internally to the pet food preparation, by mixing it with other pet food
ingredients, before further processing steps for obtaining the final pet food product
(including thermal treatment and/or extrusion and/or retorting, etc).
[0083] The term "single package" means that the components of a kit are physically associated
in or with one or more containers and considered a unit for manufacture, distribution,
sale, or use. Containers include, but are not limited to, bags, boxes, cartons, bottles,
pouches, packages of any type or design or material, over-wrap, shrink-wrap, stapled
or otherwise affixed components, or combinations thereof. A single package may be
containers of individual components physically associated such that they are considered
a unit for manufacture, distribution, sale, or use.
[0084] As used herein, a "means for communicating information or instructions" is a kit
component under any form suitable for providing information, instructions, recommendations,
and/or warranties, etc. Such a means can comprise a document, digital storage media,
optical storage media, audio presentation, visual display containing information.
The means of communication can be a displayed web site, brochure, product label, package
insert, advertisement, visual display, etc.
DESCRIPTION OF THE INVENTION
[0085] It is shown herein that pet food palatability can be advantageously enhanced upon
appropriately selecting conditions for producing animal digests by enzymatically hydrolyzing
animal viscera. These conditions include at least one of the following parameter:
enzyme amount, hydrolysis duration, target DH value. Preferably, all these 3 parameters
are appropriately selected for achieving advantageous levels of pet food palatability.
[0086] In a first aspect illustrated by Fig. 1, the present invention concerns a method
for preparing an animal digest having enhanced palatability, comprising:
- a) providing animal viscera;
- b) contacting said animal viscera with at least one alkaline endopeptidase;
- c) allowing said alkaline endopeptidase to hydrolyze said animal viscera;
- d) thermally treating the thus obtained digest product to inactivate said alkaline
endopeptidase; and
- e) obtaining said animal digest having enhanced palatability,
wherein:
- (i) (see Fig. 2A) if said alkaline endopeptidase is used in an amount (E) from about
0.017 to 0.682 % relative to the weight of the digest product obtained after step
d):
- said hydrolysis in step c) is performed during a period of time (T) from about 1.5
to about 5.0 hours; and
- the digest product obtained after step d) has a degree of hydrolysis (DH) from about
45 to about 70 %, said DH being defined by equation (1):

- (ii) (see Fig. 2B) if said alkaline endopeptidase is used in an amount (E) from 0.717
to about 1.137 % relative to the weight of the digest product obtained after step
d):
- said hydrolysis in step c) is performed during a period of time (T) from about 0.25
to about 4.0 hours; and
- the digest product obtained after step d) has a degree of hydrolysis (DH) from about
45 to about 70 %, said DH being defined by equation (2):

- (iii) if said alkaline endopeptidase is used in an amount (E) between 0.682 and 0.717
% relative to the weight of the digest product obtained after step d):
- said hydrolysis in step c) is performed during a period of time (T) from about 1.5
to about 4.0 hours; and
- the digest product obtained after step d) has a degree of hydrolysis (DH) preferably
from about 50 to about 70 %.
[0087] The method according to the present invention further comprises a step a1) after
said step a), of adjusting the pH of the animal viscera (Fig. 1). Said adjusted pH
value depends on the alkaline endopeptidase used in the method of the invention. It
is chosen in order to favor, or even optimize, the hydrolyzing activity of the enzyme.
Preferably, said step a1) is performed so as to adjust the pH to a pH value which
is the optimal pH value or pH range according to the enzyme manufacturer's recommendations.
That will be readily apparent to those skilled in the art. The pH can be adjusted
by any appropriate compound that is acceptable for use in pet food, such as phosphoric
acid, caustic soda, other conventional and appropriate acidity or basicity regulators,
and combinations thereof.
[0088] Said step c) of hydrolysis is preferably performed at a temperature which is the
optimal temperature value or temperature range according to the enzyme manufacturer's
recommendations. This belongs to the normal skills in the art. Typically, the temperature
in step c) is from about 50 to about 80°C, preferably from about 55 to about 75°C,
yet preferably from about 60 to about 70°C.
[0089] To inactivate the alkaline endopeptidase, said thermal treatment of step d) is preferably
performed at a temperature from about 80 to about 110°C, during a period of time from
about 5 to about 60 minutes. Yet preferably, said temperature is from about 90 to
about 100°C, and/or said a period of time is from about 15 to about 45 minutes.
[0090] Said step d) of heat inactivation of the enzyme is advantageously adapted to facilitate
one or more thermal reactions in the digest product. Under these circumstances, it
is an essential embodiment of the method of the present invention to further perform
a step c1) of adding one or more Maillard ingredients to the digest product of said
step c). For example, carbohydrate(s) and/or nitrogen compound(s) is(are) added at
a concentration of about 0.01 to 30%, preferably 0.1 to 20%, more preferably 0.1 to
15% for the former, and from about 0.01 to 30%, preferably 0.01 to 20%, more preferably
0.01 to 15% for the latter.
[0091] When said step d) is both to inactivate the enzyme and to allow thermal reaction(s)
to occur, an appropriate temperature is chosen in the range of about 70 to about 130°C,
preferably of about 75 to about 125°C, yet preferably of about 80 to about 120°C.
This thermal treatment is performed during a time sufficient for further developing
flavour of the digest product, e.g., during a period of time from about 15 minutes
to about 20 hours, preferably from about 20 minutes to about 10 hours, yet preferably
30 minutes to about 6 hours.
[0092] Preferably, the method according to the present invention further comprises a step
d1) after said step d), of filtrating the resulting digest product (Fig. 1). Filtration
can be performed using a conventional filter device (such commercial rotary filters).
Advantageously, said filtration is performed under appropriate conditions in order
to remove from the digest product, particles having a diameter equal to or greater
than about 500µm, preferably greater than about 400µm.
[0093] Preferably, the method according to the present invention further comprises a step
d2) of cooling down the digest product resulting from step d) if no step d1) is performed
or if steps d1) and d2) are performed concomitantly (Fig. 1). Alternatively, if step
d1) is performed after step d) and as a separate step, then step d2) consists of cooling
down the digest product resulting from said step d1). According to an embodiment,
cooling down is performed to reach a temperature less than or equal to about 100°C
(preferably, from about 80 to about 99°C) for a dry digest product. According to another
embodiment, cooling down is performed to reach a temperature less than or equal to
about 45°C (preferably, from 25 to 40°C) for a liquid digest product.
[0094] According to the definition of the term "percentage" given above, the enzyme amount
E will be expressed relative to the weight of the digest product obtained from step
d), and the DH will be measured on this digest product if steps d1) and d2) are not
performed. Alternatively, if both steps d1) and d2) are performed, the E value will
be expressed relative to the weight of the digest product obtained at the end of step
d2) (that can be concomitant with step d1)), and the DH will be measured on this digest
product. Yet alternatively, if only one step d1) or d2) is performed, the E amount
will be expressed relative to the weight of the digest product obtained at the end
of said performed step d1) or d2), and the DH will be measured on this digest product.
[0095] Preferably, the method according to the present invention further comprises a step
d3) consisting of adding one or more pet food ingredients as defined above to the
digest product resulting from:
- step d) if steps d1) and d2) are not performed after step d); or
- step d1) if only this step is performed after step d); or
- step d2) in the other cases (step d2) being possibly performed concomitantly with
step d1)) (Fig. 1).
[0096] In one embodiment, the method of the present invention further comprises a step d4)
of concentrating the digest product resulting from:
- step d) if steps d1), d2) and d3) are not performed after step d); or
- step d1) if only this step is performed after step d); or
- step d2) if only this step is performed after step d) or if only both steps d1) and
d2) are performed after step d) (step d2) being possibly concomitant with step d1));
or
- step d3) in the other cases (Fig. 1).
[0097] The concentration step d4) can be performed using conventional means. For example,
one may use commercial devices (e.g., concentrators). Alternatively, one may add to
the digest product, one or more carriers as defined above in appropriate proportions.
Concentration is advantageously performed so as to achieve a dry matter content from
about 5 to about 80%, preferably from about 10 to about 70%, yet preferably from about
20 to about 60%, by weight of the concentrated digest product.
[0098] When either step d) or d1) or d2) or d3) or d4) is followed by step e), then the
method advantageously comprises a step d5) prior to said step e), said step d5) consisting
of freezing the digest product resulting from the latter step of steps d), d1), d2),
d3), and d4) (Fig. 1). Freezing is typically performed as rapidly as possible to reach
a core temperature of about -20°C. Conventional freezing devices can be used, such
as plate deep-freezers.
[0099] In one embodiment, the method of the present invention further comprises a step d6)
of drying the digest product resulting from:
- step d) if steps d1), d2), d3), and d4) are not performed after step d); or
- step d1) if only this step is performed after step d); or
- step d2) if only this step is performed after step d) or if only both steps d1) and
d2) are performed after step d) (step d2) being possibly concomitant with step d1));
or
- step d3) if it is the only step performed after step d) or after step d1) or after
step d2) (step d2) being possibly concomitant with step d1)); or
- step d4) in the other cases (Fig. 1).
[0100] The drying step d6) is performed so as to remove any excess water. In particular,
the resulting water content is less than or equal to about 10%, preferably from about
1 to about 8%, by weight of the thus obtained dry digest product. For example, a dry
digest product is obtained by combining the digest product resulting from step d)
or d1) or d2) or d3 or d4), with carriers as defined above in appropriate proportions,
and by blending the components. The mixture is then dried by evaporation, and a dry
digest product is obtained.
[0101] In particular, when the method according to the invention comprises at least steps
a), a1), b), c), c1), d) and e), and optionally at least one step selected from d1),
d2), d3), and d4), but no steps d5) and d6), the thus obtained animal digest having
enhanced palatability is liquid (Fig. 1). Obviously, to obtain a liquid animal digest
having enhanced palatability, the method can comprise any step except the freezing
step d5) and the drying step d6). Preferably, to obtain a liquid animal digest having
enhanced palatability, the method does not comprise steps d4), d5) and d6). Yet preferably,
to obtain a liquid animal digest having enhanced palatability, the method comprises
steps a), a1), b), c), c1), d), d1), d2), d3), and e), and does not comprise steps
d4), d5) and d6). Even more preferably, to obtain a liquid animal digest having enhanced
palatability, the method consists of steps a), a1), b), c), c1), d), d1), d2), d3),
and e).
[0102] Yet in particular, when the method according to the invention comprises at least
said steps a), a1), b), c), c1),d), d5), and e), and optionally at least one step
selected from d1), d2), d3), and d4), but no step d6), the thus obtained animal digest
having enhanced palatability is frozen (Fig. 1). Obviously, to obtain a frozen animal
digest having enhanced palatability, the method comprises the freezing step d5) and
does not comprise step d6). Preferably, to obtain a frozen animal digest having enhanced
palatability, the method comprises steps a), a1), b), c), c1), d), d1), d2), d3),
d4), d5), and e), and does not comprise step d6). Yet preferably, to obtain a frozen
animal digest having enhanced palatability, the method consists of steps a), a1),
b), c), c1), d), d1), d2), d3), d4), d5), and e).
[0103] Yet in particular, when the method according to the invention comprises at least
said steps a), a1), b), c), c1), d), d6), and e), and optionally at least one step
selected from d1), d2), d3), and d4), but no step d5), the thus obtained animal digest
having enhanced palatability is dry (Fig. 1). Obviously, to obtain a dry animal digest
having enhanced palatability, the method comprises the drying step d6) but no step
d5). Preferably, to obtain a dry animal digest having enhanced palatability, the method
comprises steps a), a1), b), c), c1), d), d1), d2), d3), d4), d6), and e), and does
not comprise step d5). Yet preferably, to obtain a dry animal digest having enhanced
palatability, the method consists of steps a), a1), b), c), c1), d), d1), d2), d3),
d4), d6), and e).
[0104] The animal digest having enhanced palatability according to the present invention
(as obtained in said step e)) fulfills the above definition for a PE. This animal
digest may be directly used as it is, typically at a rate of about 0.01 to about 80%,
preferably of about 0.01 to about 60%, more preferably of about 0.01
to about 40%, even more preferably of about 0.01 to about 20%, by weight of the final
pet food. Alternatively, it may be combined with one or more other palatability-enhancing
composition ingredients, in particular other PEs, and all ingredients or all PEs may
be applied concomitantly or sequentially.
[0105] In the method of the present invention, alkaline endopeptidases are used. A more
particularly appropriate endopeptidase for use herein is an alcalase-type protease.
Non-limiting examples of commercially-available enzymes that can be used here are:
Alcalase (Novozymes, Bagsvaerd, DK), Protex
® (Danisco Genencor, Hanka, FI), Food Pro
® Alkaline (Danisco Genencor), Protemax (Prozyn, Sao paulo, BR), and Proleather (Amano,
Nishiki, JP).
[0106] Advantageous embodiments of the method of the invention are such that:
- in i):
- said amount E is from about 0.02 to 0.682%, preferably from about 0.03 to 0.682%,
yet preferably from about 0.05 to 0.682%, relative to the weight of the digest product
obtained after step d); and/or
- said period of time T is from about 1.5 to about 4 hours, preferably from about 1.5
to about 3.5 hours, yet preferably from about 1.5 to about 3 hours; and/or
- said DH is from about 50 to about 70%, preferably from about 55 to about 65%;
- in ii):
- said amount E is from 0.717 to about 1.12%, preferably from 0.717 to about 1.1%, yet
preferably from 0.717 to about 1.05%, relative to the weight of the digest product
obtained after step d); and/or
- said period of time T is from about 0.5 to about 3.5 hours, preferably from about
1 to about 3 hours, yet preferably from about 1 to about 2.5 hours; and/or
- said DH is from about 50 to about 70%, preferably from about 55 to about 65%;
- in iii):
- said period of time T is from about 1.5 to about 3.5 hours, preferably from about
1.5 to about 3 hours, yet preferably from about 2 to about 3 hours; and/or
- said DH is from about 55 to about 70%, preferably from about 55 to about 65%.
[0107] In the present method, the DH value is determined using an OPA (o-phthaldialdehyde)-based
method such as that described in the Examples below.
[0108] Preferably, viscera used in the method of the invention are selected from viscera
of poultry, pork, beef, lamb, sheep, fish, and combinations thereof. Fish viscera
are more preferably selected from viscera of tuna, salmon, cod, hake, sardine, shrimp,
squid, and combinations thereof.
[0109] The present disclosure relates to an animal digest having enhanced palatability that
is obtainable by a method as described herein. In particular, this animal digest is
dry or liquid or frozen.
[0110] Yet another aspect of the present disclosure concerns a palatability-enhancing composition
for pet food comprising at least one animal digest having enhanced palatability as
disclosed above, and one or more other palatability-enhancing composition ingredients
as defined above, such as, in particular, Maillard-reaction resulting products as
described above and/or inorganic phosphate compounds and/or microbial proteins and/or
animal proteins and/or vegetable proteins and/or carbohydrates.
[0111] The content of Maillard-reaction resulting products in said palatability-enhancing
composition is preferably of about 0.01 to 99%, yet preferably about 0.05 to 95%,
more preferably about 0.1 to 90%, yet more preferably about 0.2 to 85%, and even more
preferably about 0.5 to 80%, by weight of the composition.
[0112] In the palatability-enhancing composition provided herein, said inorganic phosphate
compound is preferably present in an amount of about 0.01 to 75%, yet preferably about
0.05 to 70%, more preferably about 0.1 to 65%, yet more preferably about 0.25 to 60%,
by weight of the composition.
[0113] Said inorganic phosphate compound is preferably selected from the group consisting
of phosphoric acid, pyrophosphates, monophosphates, polyphosphates, and combinations
thereof.
[0114] A preferred inorganic phosphate compound according to the present invention is a
pyrophosphate compound selected from disodium pyrophosphate, trisodium pyrophosphate,
tetrasodium pyrophosphate, dipotassium pyrophosphate, tripotassium pyrophosphate,
tetrapotassium pyrophosphate, tetraferric pyrophosphate, and combinations thereof.
A more particularly preferred pyrophosphate compound is trisodium pyrophosphate.
[0115] A preferred polyphosphate compound for use in the present invention is sodium tripolyphosphate.
[0116] The palatability-enhancing composition according to the invention can be dry or liquid
or frozen.
[0117] Yet another aspect herein disclosed is related to a method for enhancing the palatability
of a pet food or, in other words, for producing a pet food having enhanced palatability,
wherein said method comprises:
- a) adding to a pet food preparation or mixture, an animal digest having enhanced palatability
and/or a palatability-enhancing composition as defined above; and
- b) obtaining a pet food having enhanced palatability.
[0118] Dry pet foods such as kibbles can commonly be prepared by different methods. One
of these methods, that is widely used, is a cooker-extruder method. In the cooker-extruder
method, ingredients are first blended together to form an admixture. This admixture
is transferred into a steam conditioner where it is sufficiently moistened to become
extrudable. The admixture then enters a cooker-extruder where it is cooked at an elevated
temperature and pressure and then forced out of the apparatus through a die. This
die forms the extruder product into a specific shape. Individual pieces of food are
created by periodically slicing off the end of the extruded stream of product. The
individual pieces are then dried in a hot air dryer. Generally, the product is dried
until it contains less than 15% moisture, and preferably about 4 to 10% moisture.
The dried particles or pieces are then transferred by bulk conveyor to a coating drum
and sprayed with fat. Other liquids, such as, for example, phosphoric acid may alternatively
be applied to the pieces, or applied in addition to the fat. The resulting pellets
or kibbles constitute the basal pet food preparation, the palatability of which will
be enhanced using the animal digests having enhanced palatability and/or the palatability-enhancing
compositions of the present invention.
[0119] Moist pet foods that are gravy-based or jelly-based can be prepared by grinding meat,
meat mimetics, meat by-products, carbohydrates and/or grains, texturing agents, and
forming the ground mixture via low pressure extrusion, then cooking through a steaming
tunnel. At the tunnel outlet, the mixture is cut into pieces. The gravy- or jelly-type
matrix is added to the resulting pieces, then sealed in cans or pouches and retorted,
so as to obtain chunks-in gravy or chunks-in jelly food products.
[0120] Moist pet foods that are not gravy-based or jelly-based can be prepared by grinding
meat, meat mimetics, meat by-products, carbohydrates and/or grains, and mixing with
water and texturing agents. Then, the overall mixture is sealed in cans and retorted,
so as to obtain loaves.
[0121] The addition step a) mentioned above can thus be performed, depending on the pet
foods, animal digests having enhanced palatability and/or palatability-enhancing compositions,
either by incorporating or including said animal digests having enhanced palatability
and/or said palatability-enhancing composition into the pet food preparations or mixtures,
or by coating said pet food preparations or mixtures with said animal digests having
enhanced palatability and/or said palatability-enhancing compositions.
[0122] For example, one can cite a method for coating dry pet foods such as kibbles. Kibbles
of uncoated, extruded basal pet food can be placed in a container such a tub or a
coating drum for mixing. A fat, such as pork fat or poultry fat, is heated and then
sprayed onto the pet food in a manner to obtain a coating of the kibbles. The coating
need not be a continuous layer, but preferably is uniform. After the fat, a palatability-enhancing
composition may be applied as either a liquid or a dry powder, while the product is
mixing. A liquid animal digest having enhanced palatability and/or a liquid palatability-enhancing
composition is typically sprayed on while a dry animal digest having enhanced palatability
and/or a dry palatability-enhancing composition is typically dusted on. Alternatively,
animal digests having enhanced palatability and/or palatability-enhancing compositions
can be mixed with the fat and applied concurrently. Yet alternatively, animal digests
having enhanced palatability and/or palatability-enhancing compositions are coated
before deposition of fat.
[0123] Alternatively, the animal digest having enhanced palatability and/or the palatability-enhancing
composition can be incorporated or included into the pet food preparation according
to the following method. The animal digest having enhanced palatability and/or the
palatability-enhancing composition is contacted with the raw ingredients of the pet
food preparation prior to cooking. In this case, the animal digest having enhanced
palatability and/or the palatability-enhancing composition is combined to proteins,
fibre, carbohydrates and/or starch, etc., of the basal food preparation and is cooked
with those materials in the cooker-extruder.
[0124] Inclusion into moist pet foods can be achieved as follows. The liquid or dry or frozen
animal digest having enhanced palatability and/or the liquid or dry or frozen palatability-enhancing
composition can be applied in a gravy- or jelly-type matrix during the blending process
in addition to the other pet food ingredients. The liquid or dry or frozen animal
digest having enhanced palatability and/or the liquid or dry or frozen palatability-enhancing
composition can also be applied into a meat-by mixtures for chunks or loaf preparation.
In this case, it can be added to raw materials before or after the grinding process.
The meat-by mixture may be cooked in a steam or grilling oven in the case of chunks
manufacturing, or directly sealed in cans in the case of loaf manufacturing.
[0125] The PEs of the present invention are useful in pet foods such as nutritionally-balanced
mixtures containing appropriate pet food ingredients including proteins, fibre, carbohydrates
and/or starch, etc. Such mixtures are well known to those skilled in the art, and
their composition depends on many factors such as, for example, the desired food balance
for the specific type of pet. Additional pet food ingredients may include vitamins,
minerals, seasonings, preservatives, and surfactants. The food balance, including
the relative proportions of vitamins, minerals, lipids, proteins and carbohydrates,
is determined according to the known dietary standards in the veterinary field, for
example by following recommendations of the National Research council (NRC), or the
guidelines of the American Association of Feed Control Officials (AAFCO).
[0126] It is further herein described a pet food having enhanced palatability comprising
a pet food mixture and at least one animal digest having enhanced palatability and/or
at least one palatability-enhancing composition as described above.
[0127] For instance, said pet food is obtainable by the foregoing method of preparation.
[0128] Said pet food can be selected from wet nutritionally-balanced pet foods, dry nutritionally-balanced
pet foods, semi-moist nutritionally-balanced pet foods, supplements; treats, and toys.
[0129] Wet nutritionally-balanced pet foods can be selected from the group consisting of:
chunks-in-jelly food products, chunks-in-gravy food products, loafs, and soups.
[0130] Dry nutritionally-balanced pet foods can be kibbles.
[0131] Said pet food can be a cat food or a dog food.
[0132] It is also disclosed herein a method for feeding pets comprising at least:
- a) providing a pet food as disclosed above; and
- b) feeding said pet food to pets.
[0133] Said pets can be selected from the group consisting of cats and dogs.
[0134] Yet a further aspect of the present disclosure is a kit for enhancing the palatability
of a pet food comprising, in one or more containers in a single package:
- at least one animal digest having enhanced palatability and/or at least one palatability-enhancing
composition as described above;
- optionally, at least one pet food ingredient;
- optionally, a means for communicating information about or instructions for using
said animal digest having enhanced palatability and/or said palatability-enhancing
composition and, optionally, said pet food ingredient.
[0135] The above-described animal digests having enhanced palatability and palatability-enhancing
compositions provide significant advantages over the prior art. The effects of the
present invention can be measured by a test that is commonly called "two-bowl test"
or "versus test". Of course, the person skilled in the art is free to use any other
appropriate test than the two bowl test hereunder described to determine preference.
Such alternative tests are well known in the art.
[0136] The present invention will be further described by reference to the following examples,
which are presented for the purpose of illustration only and are not intended to limit
the scope of the invention.
EXAMPLES
A- DH measurement method (described in Nielsen et al, 2001):
[0137] In protein hydrolysates, the key parameter for monitoring the reaction is the degree
of hydrolysis (DH). DH is defined as the percentage of cleaved peptide bonds:

where h
tot is the total number of peptide bonds per protein equivalent, and h is the number
of hydrolyzed bonds. h is expressed in equivalent of serine-NH
2, as serine shows a response close to the average of all amino acids according to
the formula:

[0138] Most of food proteins have an average value of 125g/mol of amino acid molecular weight,
that gives a h
tot = 8, can be adapted to the value of 7.6 for meat and 8.6 for fish. α and β values
are set at 1.00 and 0.40 for meat and fish, respectively.
A-1-Principle:
[0139] Each hydrolysed peptide bond lead to a free amino group. Those amino groups react
with OPA to form a yellow complex that will then be measured in spectrophotometry
at 340 nm. The optical density is a function of the complex numbers.
[0140] The method consists then of measuring the h value, then the serine equivalent value
of the hydrolysate and of comparing the coloring complex formed in the hydrolysates
reported to the level of complex formed in a serine standard (with the correction
of a blank).
A-2- Apparatus:
[0141] Erlenmeyer flasks, 4-decimal analytical balance. Pipettes: adapted to the volume.
Magnetic stirrer, vortex, Spectrophotometer at 340 nm.
A-3- Reagents:
[0142] The OPA reagent was prepared as follows in a 200 ml flask: 7.620 g di-Natetraborate
decahydrate and 200 mg Na-dodecyl-sulfate (SDS) were dissolved in 150 mL deionized
water. The reagents have to be completely dissolved before continuing. 160 mg OPA
97% was dissolved in 4 mL ethanol. The OPA solution was then transferred quantitatively
to the above mentioned solution by rinsing with deionized water. 176 mg dithiothreitol
99% (DTT) was added to the solution by rinsing with deionized water. The solution
was made up to 200 mL with deionized water.
[0143] The serine standard was prepared by dissolving 50 mg serine in 500 mL deionized water
(0.9516 meqv/L).
[0144] The sample solution was prepared by dissolving 200 mg in 100 mL deionized water.
A-4- Measurements:
[0145] 3 ml of OPA was put in each of the 6 micro spectrotube. Then, 400 µL of water (Blank),
serine standard or sample is added, and measurement done at the same + 2 minutes reacting
time. For each sample, a blank, then 2 standard measurements, then 3 sample measurements
were done.
[0146] Assays were realized at 20°C.
Typical absorbance readings for the standards and water blanks are 0.8 and 0.07, respectively.
A-5- Determination of h and DH:
[0147]
where serine-NH2 = meqv serine NH2/g protein; X = g sample; P = protein % in sample; 0.1 is the sample volume in liter
(L).
h is then: h = (serine-NH2 - β)/α meqv/g protein, where α and β are given above.
Calculation of DH: DH = h / htot x 100 %.
B- Palatability assessment using the "two-bowl" test:
B-1- Principle of the two-bowl test:
[0148] The test is based on the postulate whereby the more food consumed, the more palatable
it is.
[0149] Individual versus (Two bowls) appetence tests, based on the comparison between two
foods, were carried out. Tests are performed either on panel of 36 dogs or on panel
of 40 cats, depending on the test's objectives.
B-2- Operating method of the test:
[0151] Cat test: The bowls were presented at the same time to each cat in an individual
loose box and their positions were switched at each meal to avoid a choice led by
handedness.
- Duration of the test:
* Cat test for dry food: from about 15 minutes to about 20 hours (if one of the two
bowls was entirely eaten before the end of the test, the two bowls were removed, and
the test was stopped);
* Cat test for wet food: from about 15 minutes to about 30 minutes (if one of the
two bowls was entirely eaten before the end of the test, the two bowls were removed,
and the test was stopped);
* Dog test: from about 15 minutes to about 30 minutes (if one of the two bowls was
entirely eaten before the end of the test, the two bowls were removed, and the test
was stopped). Parameters studied
- Measured parameters: First food consumed ("initial appeal") and amount of each food
consumed by the end of the test;
- Calculated parameters: individual consumption ratio in % (CR)


[0152] 
Average consumption ratio (ACR) = average of all individual ratios (an equal importance
is given to each animal, regardless of its size and of its corresponding consumption).
[0153] If animals have higher or lower consumption compared to predetermined values (which
are function of, e.g., the animal weight and/or metabolism), they are not taken into
account into statistical treatment.
B-3- Statistical analysis:
[0154] Statistical analysis was used to determine if there was a significant difference
between the 2 ratios. A Student's t-test with 3 error thresholds, namely 5%, 1% and
0.1% was performed.
[0155] A Chi-square test was used to determine if there was a significant difference between
the number of pets with Food A as first food eaten and the number of pets with Food
B as first food eaten.
[0156] Significance levels are noted as below:
| NS |
not significant |
(p > 0.05) |
| * |
significant |
(p < 0.05) |
| ** |
highly significant |
(p < 0.01) |
| *** |
very highly significant |
(p < 0.001) |
C- Examples of embodiments of the present invention:
[0157] The examples disclosed herein to illustrate the present invention refer to two palatability
positioning.
[0158] In Example 1, variations of the 3 following parameters: alkaline endopeptidase amounts
(E), hydrolysis time (T), and DH values, allowed to obtain different animal digests
that were compared for their palatability.
[0159] In Examples 2 to 4, one particular combination of an alkaline endopeptidase amount
E and a hydrolysis time T of animal viscera was chosen and compared in palatability
testing to similar animal digests obtained using a neutral endopeptidase.
Example 1:
[0160] In this example, different dry animal digests were prepared according to different
conditions of hydrolysis. All dry animal digests were prepared according to Fig 1.
The formulation of liquid digest product A is described in the Table 1 below:
Table 1
| Formulation of liquid digest product A |
% by weight of liquid digest product A |
| Poultry livers |
92.0 |
| Caustic soda |
4.09 |
| Antioxydants |
0.15 |
| Citric acid |
0.03 |
| Ascorbic acid |
0.02 |
| Maillard Ingredients |
3.4 |
| Enzyme: Alkaline endopeptidase |
0.31 |
[0161] Liquid digest product A ("Liq dig pd A") was prepared as follows. Fresh raw materials
(poultry livers) were ground in a vertical cutter for 2 min at a maximum speed. The
ground raw materials were transferred to a reactor and mixed with the other ingredients.
pH was adjusted at 8.5 with caustic soda, and then enzyme was incorporated. The hydrolysis
step was carried at 60°C for 3 hours. At the end of the hydrolysis step, Maillard
ingredients were incorporated. The temperature was gradually increased to 100°C and
maintained for 30min in order to inactivate the enzyme, to allow Maillard reaction
and thus to develop flavour compounds. A slight cooling was set before beginning a
rough filtration to obtain a liquid digest product A with a particle size lower than
500 µm.
[0162] This liquid was then spray dried at appropriate temperature from 180 to 220°C for
several minutes, in order to remove excess of water. Dry animal digest A was thus
obtained.
[0163] The formulation of liquid digest products B, C, O, E, F, G, and H is similar to that
of liquid digest product A, except (see Table 2 below) the amount of alkaline endopeptidase
E (%) and the duration of hydrolysis (hours).
[0164] Variations of the amount of enzyme were compensated by more or less ground poultry
liver.
Table 2
| |
Alkaline endopeptidase (%) |
Hydrolysis time (h) |
DH (%) |
| Liq Dig Pd A |
0.31 |
3 |
60.8 |
| Liq Dig Pd B |
1.085 |
2 |
60.8 |
| Liq Dig Pd C |
0.93 |
0.5 |
49.1 |
| Liq Dig Pd D |
0.15 |
1 |
37.2 |
| Liq Dig Pd E |
1.137 |
1 |
50.3 |
| Liq Dig Pd F |
1.137 |
2 |
64.6 |
| Liq Dig Pd G |
1.137 |
3 |
68.7 |
| Liq Dig Pd H |
1.225 |
2 |
62 |
[0165] DH values were determined as in all examples herein disclosed, i.e., after the thermal
treatment for inactivating the enzyme as described above (see Fig. 1). Liquid digest
products A, B, C, D, E, F, G, and H are spotted in Fig. 2A and 2B.
[0166] Dry animal digests B, C, D, E, F, G, and H were obtained from liquid digest products
B, C, D, E, F, G, and H, respectively, as described above in connection with dry animal
digest A.
[0167] Palatability assessment: Compositions A, B, C, D, E, F, G, and H were obtained after blending dry animal digests
A, B, C, D, E, F, G, and H, respectively, each with trisodium pyrophosphate in a respective
proportion of 60:40, and dusted at 1.5% by weight of dry cat kibbles previously coated
with 6% of poultry fat, giving complete and nutritionally-balanced palatable dry cat
foods A, B, C, D, E, F, G, and H.
[0168] Palatability was assessed as described above in order to compare cat food products
C, D, E, F, G, and H to A. In addition, palatability of cat food product H was compared
to that of cat food product B.
[0169] Results of palatability for average consumption ratio (in %) for Day 1 and Day 2
are presented below in Tables 3A and 3B:
Table 3A
| |
DAY 1 |
DAY 2 |
| Test of petfood |
Average consumption of dry cat food A (%) |
Average consumption of the dry cat food compared to A (%) |
Statistical Significance |
Average consumption of dry cat food A (%) |
Average consumption of the dry cat food compared to A (%) |
Statistical Significance |
| A vs C |
59 |
41 |
NS |
45 |
55 |
NS |
| AvsD |
62 |
38 |
** |
58 |
42 |
* |
| A vs E |
40 |
60 |
* |
43 |
57 |
NS |
| A vs F |
53 |
47 |
NS |
54 |
46 |
NS |
| AvsG |
47 |
53 |
NS |
50 |
50 |
NS |
| A vs N |
65 |
35 |
*** |
64 |
36 |
** |
Table 3B
| |
DAY 1 |
DAY 2 |
| |
Average consumption of dry cat food B (%) |
Average consumption of dry cat food H (%) |
Statistical significance |
Average consumption of dry cat food B (%) |
Average consumption of dry cat food H (%) |
Statistical Significance |
| B vs H |
63 |
37 |
*** |
64 |
36 |
** |
[0170] Those results show that food products C, E, F, and G had equivalent palatability
compared to food product A, whereas (i) food product D had inferior palatability than
food product A and (ii) food product H had inferior palatability than food products
A and B, demonstrating that specific hydrolysis conditions enable to increase cat
food palatability.
Example 2:
[0171] Two dry animal digests for cats were manufactured as follows:
Composition 1:
[0172] Formulation is expressed by weight of the liquid digest product:
Table 4
| Formulation of liquid digest product 1 |
% by weight of liquid digest product 1 |
| Pork liver |
92.32 |
| Caustic soda |
3.7 |
| Antioxydants |
0.15 |
| Citric acid |
0.03 |
| Ascorbic acid |
0.02 |
| Maillard Ingredients |
3.4 |
| Enzyme: Neutral endopeptidase |
0.384 |
[0173] Fresh raw materials (pork livers) were ground in a vertical cutter for 2 min at a
maximum speed. The ground raw materials were transferred to a reactor and mixed with
the other ingredients. pH was adjusted to 6.5 with caustic soda, and then enzyme was
incorporated. The hydrolysis step was carried at 55°C for 3 hours. At the end of the
hydrolysis step, Maillard ingredients were incorporated. The temperature was gradually
increased to 100°C and maintained during 30min in order to inactivate the enzyme,
to allow Maillard reaction, and thus to develop flavour compounds. A slight cooling
was set before beginning a rough filtration to obtain a liquid digest product 1 with
a particle size lower than 500 µm.
[0174] This liquid was then spray dried at appropriate temperature from 180 to 220°C for
several minutes, in order to remove excess of water. Dry animal digest 1 was obtained.
A cat powder composition 1 was then obtained by blending 60% of dry animal digest
1 with 40% of trisodium pyrophosphate.
Composition 2:
[0175] The formulation of liquid digest 2 is the same as the formulation of liquid digest
1, except the enzyme used that was an alkaline endopeptidase. Manufacturing conditions
were the same, excepting that pH and temperature were adjusted according to the enzyme
supplier's recommendations, respectively 8.5 and 60°C. A cat powder composition 2
was thus obtained.
Table 5
| Formulation of liquid digest product 2 |
% by weight of liquid digest product 2 |
| Pork liver |
92.32 |
| Caustic soda |
3.70 |
| Antioxydants |
0.15 |
| Citric acid |
0.03 |
| Ascorbic acid |
0.02 |
| Maillard Ingredients |
3.4 |
| Enzyme: Alkaline endopeptidase |
0.384 |
[0176] DH values were measured as described above. Results are reported in Table 6 below.
Table 6
| |
Liquid digest product 1 |
Liquid digest product 2 |
| DH % |
36.2 |
60.3 |
[0177] Cat powder composition 1 or 2 was dusted at 1.5% by weight of dry cat kibbles previously
coated with 6% of poultry fat. The two pet foods, cat food 1 and cat food 2, were
presented to cats for palatability assessment as described above. 5
Table 7: Cat palatability results
| |
DAY 1 |
DAY 2 |
| |
Average consumption cat food 1 (%) |
Average consumption cat food 2 (%) |
Statistical significance |
Average consumption cat food 1 (%) |
Average consumption cat food 2 (%) |
Statistical Significance |
| 1st choice |
36 |
64 |
NS |
26 |
64 |
** |
| Consumption |
34.5 |
65.5 |
*** |
37 |
63 |
** |
[0178] As shown in Table 7, consumption of food was significantly different between cat
food 1 and cat food 2, demonstrating the higher palatability for cats of a digest
obtained by using an alkaline endopeptidase compared to one obtained using a neutral
endopeptidase.
Example 3:
[0180] Composition 3 was a premium dry cat PE of the commercial range SPF C'SENS
®, obtained by hydrolyzing poultry viscera with a neutral endopeptidase (LiquiddDigest
product 3) followed by a drying step.
Composition 4 was prepared in the same way than composition A in Example 1 above.
[0181] DH values were determined as described above. Results are shown in Table 8:
Table 8
| |
Liquid digest product 3 |
Liquid digest product 4 |
| DH % |
34.8 |
62.2 |
[0182] Composition 3 or 4 was dusted at 1.5% by weight of dry cat kibbles previously coated
with 6% of poultry fat. The two cat foods 3 and 4 were presented to cats for palatability
assessment.
Table 9
| |
DAY 1 |
DAY 2 |
| |
Average consumption cat food 3 (%) |
Average consumption cat food 4 (%) |
Statistical Significance |
Average consumption cat food 3 (%) |
Average consumption cat food 4 (%) |
Statistical Significance |
| 1st choice |
41 |
59 |
NS |
47 |
53 |
NS |
| Consumption |
36 |
64 |
** |
36 |
64 |
** |
[0183] As shown in Table 9, consumption of food was significantly different between cat
food 3 and cat food 4, demonstrating the higher palatability for cats of a digest
obtained by using an alkaline endopeptidase compared to one obtained by using a neutral
endopeptidase.
Example 4:
[0185] Liquid digest product 5 was a Premium liquid dog PE of the commercial range SPF D'TECH, obtained by hydrolyzing
pork viscera with a neutral endopeptidase.
[0186] Liquid digest product 6: The applied process was similar to the process used in Example 2 - The formulation
of liquid digest product 6 is detailed in Table 10:
Table 10
| Formulation of liquid digest product 6 |
% by weight of liquid digest product 6 |
| Pork liver&Lungs |
92.80 |
| Caustic soda |
3.22 |
| Antioxydants |
0.15 |
| Citric acid |
0.03 |
| Ascorbic acid |
0.02 |
| Maillard Ingredients |
3.4 |
| Enzyme: Alkaline endopeptidase |
0.384 |
[0187] The liquid digest product 6 was not dried in this example but cooled and stabilized
by addition of potassium sorbate, anti-oxidants and phosphoric acid, to obtain a final
liquid dog digest having a pH of 2.9.
[0188] DH was measured as described above. Results are shown in Table 11.
Table 11
| |
Liquid digest product 5 |
Liquid digest product 6 |
| DH % |
40.7 |
55.2 |
[0189] Liquid dog digest 5 or 6 was sprayed at 3% by weight of dog kibbles previously coated
with 6% of pork fat. The resulting dry dog foods 5 and 6 were presented to dogs for
palatability assessment as described above.
Table 12: Palatabitity results:
| |
DAY 1 |
| |
Average consumption dog food 4 (%) |
Average consumption dog food 5 (%) |
Statistical Significance |
| 1st choice |
24 |
76 |
** |
| Consumption |
27 |
73 |
*** |
[0190] As shown in Table 12, consumption of food was significantly different between dog
food 4 and dog food 5, demonstrating the higher palatability of a digest obtained
by using an alkaline endopeptidase compared to one obtained using a neutral endopeptidase.
REFERENCES